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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616541Generated: October 31, 2026

Ammonia → 2,2,6,6-Tetramethyl-3-(prop-2-en-1-yl)piperidin-4-one

https://huagongshe.com/reaction/616541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
Reactant5-Allyl-1,2,5,6-tetrahydro-2,2,6,6-tetramethyl-4-piperidinopyridineHCID 21330385—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2,2,6,6-Tetramethyl-3-(prop-2-en-1-yl)piperidin-4-oneHCID 2133049083.8%

Reaction Steps

1.46 g of the 5-allyl-1,2,5,6-tetrahydro-2,2,6,6-tetramethyl-4-piperidinopyridine thus obtained were dissolved in a mixture of 3 ml of acetic acid, 1.5 g of sodium acetate and 3 ml of water, and the solution was allowed to stand overnight. To the solution were then added 6.0 g of sodium bicarbonate and 3 ml of concentrated aqueous ammonia; the mixture was then extracted with hexane. The extract was dried over anhydrous magnesium sulphate and then treated with charcoal. 0.91 g of the title compound was obtained after removal of the hexane. The compound showed a single spot on thin layer chromatography using a 0.25 mm thick layer of alumina and a mixture of benzene/hexane/ethyl acetate/triethylamine (2 : 2 : 1: 0.5 by volume) as developing solvent; Rf value 0.70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04075165
Source datasetuspto-grants-1978_02
ORD IDord-9c00ef3baf0143bc8bb34f8827d70c61
Source noteuspto-grants-1978_02